Product image of Lercan (Lercanidipine Hydrochloride) supplied by GNH India

Lercan

Active Ingredient:
Lercanidipine Hydrochloride
Origin:
EU

Lercan (Lercanidipine Hydrochloride)

Lercanidipine, the active ingredient in Lercan, is a calcium channel blocker presented as an oral tablet for oral administration. It selectively relaxes vascular smooth muscle, thereby reducing peripheral vascular resistance and lowering systolic and diastolic blood pressure in adult patients diagnosed with hypertension.

GNH India supplies Lercan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing products that meet EU quality standards for global distribution. The company ensures traceability, proper documentation, and regulatory compliance for each batch.

Manufacturer / TM Owner

Bouchara Recordati

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Indications & Clinical Uses

Lercanidipine is employed in the management of hypertension, a chronic condition where persistently high arterial pressure increases the risk of heart attack, stroke, and kidney disease. By targeting vascular smooth muscle, the medication helps achieve blood pressure control.

  • Hypertension: reduces both systolic and diastolic blood pressure, lowering risk of cardiovascular events.
  • Isolated systolic hypertension: preferentially lowers systolic pressure, beneficial in older adults.

How It Works

  • Lercanidipine selectively blocks L-type calcium channels in vascular smooth muscle cells. Inhibition of calcium influx prevents contraction, causing dose‑dependent vasodilation of arterioles. The resulting decrease in peripheral vascular resistance leads to lowered arterial pressure without significant effect on heart rate or cardiac contractility. Its high lipophilicity allows prolonged action and smooth onset, contributing to once‑daily dosing. The drug is extensively metabolized by the liver, primarily via CYP3A4, and its metabolites are excreted in the urine and feces.

Side Effects

Lercanidipine may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate pain often occurring after dose initiation.
  • Flushing: transient warmth and redness of the skin.
  • Peripheral edema: swelling of the ankles or lower legs.
  • Dizziness: light‑headed sensation, especially when standing quickly.

Serious or Rare Side Effects

  • Severe hypotension: marked drop in blood pressure that may cause fainting.
  • Myocardial infarction: rare occurrence of heart attack.
  • Hepatic dysfunction: abnormal liver enzymes or hepatitis.
  • Anaphylactic reaction: life‑threatening allergy with rash, swelling, and breathing difficulty.

Precautions & Warnings

When prescribing Lercanidipine, clinicians should consider several safety measures.

  • Dose adjustment: required in patients with hepatic impairment.
  • Monitor blood pressure: check regularly after initiation or dose changes.
  • Avoid abrupt discontinuation: may cause rebound hypertension.
  • Caution in elderly: increased sensitivity to hypotensive effects.
  • Drug interactions: review concomitant medications that affect CYP3A4.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture.

Avoid Interactions

Lercanidipine can interact with several medicines, necessitating careful review.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase plasma levels, risk of hypotension.
  • Grapefruit juice: can elevate drug concentration, leading to excessive vasodilation.
  • Simultaneous use with other calcium channel blockers: additive blood pressure lowering effect.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy.
  • Diuretics: may enhance hypotensive response.
  • Beta‑blockers: combined effect on heart rate and blood pressure may require dose adjustment.

Frequently Asked Questions

Lercan contains the active ingredient lercanidipine, which is prescribed to lower elevated blood pressure in adult patients. By relaxing the smooth muscle of blood vessels, it helps achieve target blood pressure levels and reduces the risk of cardiovascular complications associated with hypertension.

Lercanidipine works by selectively inhibiting L-type calcium channels in vascular smooth‑muscle cells. This blockade prevents calcium‑induced contraction, causing vasodilation of peripheral arteries, which lowers systemic vascular resistance and consequently reduces both systolic and diastolic blood pressure.

The appropriate dose of Lercan is determined by the prescribing healthcare professional based on the individual’s blood‑pressure profile, age, renal and hepatic function, and concomitant medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for lercanidipine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their healthcare provider.

To request Lercan, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will verify trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Lercan belongs to the dihydropyridine calcium‑channel blocker class, offering once‑daily dosing and a favorable side‑effect profile compared with some older agents. Compared with beta‑blockers, it primarily reduces peripheral resistance without significantly affecting heart rate, making it a useful option for patients who cannot tolerate beta‑blockade.

Lercan tablets should be stored at ambient temperature, below 25 °C, in their original packaging to protect them from moisture and light. Keep the product out of reach of children and avoid storing in areas with high humidity or direct sunlight.

Lercan is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew it unless specifically instructed by a healthcare professional.

Serious adverse events, although rare, include severe hypotension, myocardial infarction, hepatic dysfunction, and anaphylactic reactions. Patients should seek immediate medical attention if they experience fainting, chest pain, jaundice, rash, swelling of the face or throat, or difficulty breathing.

Lercan is contraindicated in patients with known hypersensitivity to lercanidipine or any component of the formulation, and in individuals with severe aortic stenosis or cardiogenic shock. Caution is also advised for patients with significant liver impairment or those taking strong CYP3A4 inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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